@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_head
{
this:
np:hasAssertion
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_assertion
;
np:hasProvenance
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_provenance
;
np:hasPublicationInfo
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_assertion
a
np:Assertion
.
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_provenance
a
np:Provenance
.
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_assertion
{
miriam-gene:51750
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN48fd5f8962b6c5c198e4332a668bf832
sio:SIO_000628
miriam-gene:51750
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_provenance
{
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_assertion
dcterms:description
"[Taken together, these data suggest that concurrent overexpression of cyclin D1 and functional elimination of p16CDKN2 and p15CDKN2B may characterize certain cases of mantle cell NHL, and that cooperation of the abnormalities is likely to provide a growth advantage of the tumour cells through more efficient inactivation of the RB tumor suppressor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9001420
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP937248.RA6YiXtLMoY4naNB9-5Go1EgsBOiLMYa_PXWj1X0qUM4M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}